| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231707029-231707189 | Rare:37 | ||||
| chr2:231708354-231708745 | Common:3; Rare:177 | ||||
| chr2:231781247-231781426 | Rare:48 | ||||
| chr2:231786192-231786463 | Common:3; Rare:73 | ||||
| chr2:231961638-231961748 | Rare:33; Clinvar:1 | ||||
| chr2:232550545-232550727 | Rare:73 | ||||
| chr2:232550974-232551106 | Rare:24 | ||||
| chr2:232696976-232697375 | Common:4; Rare:124 | ||||
| chr2:233854431-233854775 | Common:5; Rare:99 | ||||
| chr2:236507423-236507689 | Common:7; Rare:93 | ||||
| chr2:237085803-237085979 | Common:1; Rare:72 | ||||
| chr2:237487181-237487277 | Common:1; Rare:25 | ||||
| chr2:237966728-237967078 | Common:4; Rare:108 | ||||
| chr2:238060732-238061099 | Common:6; Rare:115 | ||||
| chr2:238203591-238203830 | Common:3; Rare:108 |